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"BIOSCULPTOR" Prosthetic and orthotic accessory (Non-Sterile) - Taiwan Registration ab617195571877922c94aa1a38eebab1

Access comprehensive regulatory information for "BIOSCULPTOR" Prosthetic and orthotic accessory (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ab617195571877922c94aa1a38eebab1 and manufactured by BIOSCULPTOR CORPORATION. The authorized representative in Taiwan is COPRO ORTHOTIC DESIGN CO., LTD..

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ab617195571877922c94aa1a38eebab1
Registration Details
Taiwan FDA Registration: ab617195571877922c94aa1a38eebab1
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Device Details

"BIOSCULPTOR" Prosthetic and orthotic accessory (Non-Sterile)
TW: "็™พๅ„ชๅฒ่€ƒๆ™ฎ็‰น" ็พฉ่‚ขๅŠ่ฃๅ…ท็”จ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

ab617195571877922c94aa1a38eebab1

Ministry of Health Medical Device Import No. 015769

DHA09401576903

Company Information

United States

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Accessories for Prosthetics and Accessories for Accessories for Appliances (O.3025)".

o Equipment for physical medicine

O3025 Accessories for prosthetics and accessories

Imported from abroad

Dates and Status

Oct 22, 2015

Oct 22, 2025